VITROLIFE G-2™ - Indonesia BPOM Medical Device Registration

VITROLIFE G-2™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106704866. The device is manufactured by VITROLIFE SWEDEN AB., SWEDEN from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIPA PHARMALAB INTERSAINS.

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